
Fortrea Jobs in Canada
36 jobs at Fortrea in Canada
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Senior Regulatory Medical Writer
1 day ago
Fortrea MontrealOverview · At Fortrea, we help bring life‑changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high‑complexity clinical regulatory documents in partnership with a leading global pharmaceutical company. · ...
- Fortrea Montreal (administrative region)
A global pharmaceutical company in Montreal is seeking a Senior Regulatory Medical Writer to lead the development of clinical regulatory documents. Ideal candidates should have at least 4 years of regulatory medical writing experience and a Bachelor's degree in life sciences. Res ...
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Lead Clinical Programmer. FSP Remote Based
1 week ago
FortreaWe are seeking a Lead Clinical Programmer to join our sponsor dedicated department. As a key member of our team, you will be responsible for leading the development and implementation of SAS programming solutions to address global technical services issues and optimize clinical d ...
- Fortrea Montreal
Our FSP team is currently seeking a Sr. CRA 2 with 4+ years of monitoring as well as strong Oncology monitoring experience, residing in Alberta and Montreal, Canada. · What You Will Do · You will utilize your skills, knowledge, and clinical judgement to provide a high standard of ...
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Principal Regulatory Medical Writer
3 days ago
Fortrea Toronto, ONLead authoring and development of high- complexity clinical regulatory documents for a Top 10 global pharmaceutical company as an embedded member of their team. · ...
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Senior Regulatory Medical Writer
1 day ago
Fortrea Montreal (administrative region)Overview · At Fortrea, we help bring life‑changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high‑complexity clinical regulatory documents in partnership with a leading global pharmaceutical company. · ...
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Senior Medical Writer
1 week ago
Fortrea MontrealResponsible for preparation and coordination of clinical study protocols and clinical study reports (CSRs), and other documents as needed. · ...
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Senior Regulatory Medical Writer
3 days ago
Fortrea Toronto, ONWe help bring life-changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high-complexity clinical regulatory documents in partnership with a leading global pharmaceutical company. · You can shape your car ...
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Lead Clinical Programmer. FSP Remote Based
2 days ago
Fortrea Remote CanadaAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technolog ...
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Lead Clinical Programmer. FSP Remote Based
1 month ago
FortreaJoining Fortrea's Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. · ...
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Principal Medical Writer
4 days ago
Fortrea MontrealWe are seeking an experienced Principal Medical Writer to lead the authoring and development of high‑complexity clinical regulatory documents. · ...
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Lead Clinical Programmer. FSP Remote Based
1 month ago
Fortrea Toronto, ONWe are seeking a highly skilled Lead Clinical Programmer to join our sponsor dedicated team at Fortrea, a leading global contract research organization (CRO). · The successful candidate will have extensive experience in data management and/or database programming activities inclu ...
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Principal Biostatistician
1 month ago
Fortrea TorontoAs an experienced Principal Biostatistician in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. · ...
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Senior Medical Writer
4 days ago
Fortrea MontrealWe help bring life‑changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high‑complexity clinical regulatory documents in partnership with a leading global pharmaceutical company. · ...
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CRA II
17 hours ago
Fortrea MontrealJoin to apply for the CRA II & Sr. CRAs - Canada role at Fortrea · 4 days ago – Be among the first 25 applicants · We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team. Oncology or Ophthalmology experience is desired, and candidates from ...
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Principal Medical Writer
4 days ago
Fortrea MontrealWe are seeking an experienced Principal Medical Writer to lead the authoring and development of high-complexity clinical regulatory documents. · This is meaningful work with real impact. Your job matters at Fortrea. · ...
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CRA II
2 weeks ago
Fortrea MontrealWe are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. · CAR-T experienced Sr. CRAs located anywhere in Canada strongly desired · You will utilize your skills, knowledge, and clinical judgement to provide a hig ...
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Senior Specialist, Patient Safety Solutions
5 days ago
Fortrea MontrealFortrea is currently seeking a remote based Senior Specialist (Patient Safety Solutions) to assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical tri ...
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Senior Specialist, Patient Safety Solutions
4 days ago
Fortrea MontrealFortrea is currently seeking a remote based Senior Specialist (Patient Safety Solutions) to assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical tri ...
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Senior CRA
2 days ago
Fortrea TorontoA leading clinical research organization is seeking experienced CRAs to join their Full Service Outsourcing team in Canada. This mid-senior level role involves site monitoring, patient care, and data integrity assurance in clinical trials. Candidates with experience in oncology o ...